Zhu Xia, Li Bin, Liu Yuzhen, Chen Shujian, Ye Yangfang, Li Ronghua, Song Weiwei, Mu Changkao, Wang Chunlin, Shi Ce
Key Laboratory of Aquacultural Biotechnology, Ningbo University, Chinese Ministry of Education, Ningbo 315211, China.
Key Laboratory of Green Mariculture (Co-Construction by Ministry and Province), Ministry of Agriculture and Rural, Ningbo 315211, China.
Animals (Basel). 2025 Jun 21;15(13):1837. doi: 10.3390/ani15131837.
To investigate thermal tolerance, physiological responses, and molecular mechanisms of the narrow-clawed crayfish () under acute thermal stress, the were acutely exposed to 4 different temperature groups-15 °C (control), 20 °C (T20), 25 °C (T25), and 30 °C (T30)-across 6 time points (3 h, 6 h, 12 h, 24 h, 48 h, and 72 h). Survival rates were recorded at each interval. Subsequent analyses comprised: (1) Hemolymph biochemical parameter determination; (2) hepatopancreatic antioxidant capacity assessment; (3) hepatopancreatic histopathology; and (4) comparative transcriptomics analysis of the hepatopancreas. The results showed that the survival rate in the T30 group significantly declined after 48 h of stress. The histological analysis of the hepatopancreas revealed tissue damage in both the T25 and T30 groups. The T25 group exhibited a notable increase in B-cell density and severe vacuolization, while the T30 group displayed disorganized hepatopancreatic cell arrangement, marked necrosis, and structural phenotypes in hepatopancreatic tubules, including lumen expansion and the loss of the star-shaped lumen structure. Biochemical analyses indicated pronounced declines in energy metabolism markers under elevated temperatures. Furthermore, the T30 group exhibited elevated levels of reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT), alongside diminished total antioxidant capacity (T-AOC). Similarly, the T25 group displayed increased MDA and CAT levels but decreased T-AOC. Comparative transcriptomic analysis demonstrated that differentially expressed genes (DEGs) in the control vs. T25 group were predominantly enriched in metabolic pathways, whereas DEGs identified in control vs. T30 and T25 vs. T30 comparisons showed significant enrichment in energy metabolism and apoptotic processes. Based on these findings, we concluded that acute thermal stress induces mortality in through hepatopancreatic structural damage, energy metabolism dysregulation, and excessive ROS accumulation. Notably, should be excluded from aquaculture environments exceeding 25 °C. These results enhance understanding of the adaptive mechanisms of under acute thermal stress and provide actionable insights to advance its industrial cultivation.
为研究窄额螯虾在急性热应激下的热耐受性、生理反应和分子机制,将窄额螯虾急性暴露于4个不同温度组——15℃(对照组)、20℃(T20)、25℃(T25)和30℃(T30)——并设置6个时间点(3小时、6小时、12小时、24小时、48小时和72小时)。每个时间间隔记录存活率。后续分析包括:(1)血淋巴生化参数测定;(2)肝胰腺抗氧化能力评估;(3)肝胰腺组织病理学检查;(4)肝胰腺比较转录组学分析。结果表明,应激48小时后,T30组的存活率显著下降。肝胰腺组织学分析显示,T25组和T30组均出现组织损伤。T25组B细胞密度显著增加且出现严重空泡化,而T30组肝胰腺细胞排列紊乱,出现明显坏死,肝胰腺小管出现结构表型,包括管腔扩张和星形管腔结构丧失。生化分析表明,高温下能量代谢标志物显著下降。此外,T30组活性氧(ROS)、丙二醛(MDA)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)水平升高,总抗氧化能力(T-AOC)降低。同样,T25组MDA和CAT水平升高,但T-AOC降低。比较转录组学分析表明,对照组与T25组的差异表达基因(DEG)主要富集于代谢途径,而对照组与T30组以及T25组与T30组比较中鉴定出的DEG在能量代谢和凋亡过程中显著富集。基于这些发现,我们得出结论,急性热应激通过肝胰腺结构损伤、能量代谢失调和ROS过度积累导致窄额螯虾死亡。值得注意的是,超过25℃的水产养殖环境应排除窄额螯虾。这些结果增进了对窄额螯虾在急性热应激下适应机制的理解,并为推进其工业化养殖提供了可行的见解。